Anesthesia and Critical Care Medicine Department, Edouard Herriot Hospital, Hospices Civils de Lyon, Lyon, France.
EA 7426 "Pathophysiology of Injury-Induced Immunosuppression" (Université Claude Bernard Lyon 1 - Hospices Civils de Lyon - bioMérieux), Lyon, France.
Crit Care. 2024 Jul 8;28(1):227. doi: 10.1186/s13054-024-04998-w.
Acute kidney injury (AKI) is common in hospitalized patients and results in significant morbidity and mortality. The objective of the study was to explore the systemic immune response of intensive care unit patients presenting with AKI, especially the association between immune profiles and persistent AKI during the first week after admission following various types of injuries (sepsis, trauma, surgery, and burns).
REALAKI is an ancillary analysis of the REAnimation Low Immune Status Marker (REALISM) cohort study, in which 359 critically ill patients were enrolled in three different intensive care units. Patients with end-stage renal disease were excluded from the REALAKI study. Clinical samples and data were collected three times after admission: at day 1 or 2 (D1-2), day 3 or 4 (D3-4) and day 5, 6 or 7 (D5-7). Immune profiles were compared between patients presenting with or without AKI. Patients with AKI at both D1-2 and D5-7 were defined as persistent AKI. A multivariable logistic regression model was performed to determine the independent association between AKI and patients' immunological parameters.
Three hundred and fifty-nine patients were included in this analysis. Among them, 137 (38%) were trauma patients, 103 (29%) post-surgery patients, 95 (26%) sepsis patients, and 24 (7%) were burn patients. One hundred and thirty-nine (39%) patients presented with AKI at D1-2 and 61 (20%) at D5-7. Overall, 94% presented with persistent AKI at D5-7. Patients with AKI presented with increased pro and anti-inflammatory cytokines and altered innate and adaptive immune responses. The modifications observed in the immune profiles tended to be more pronounced with increasing KDIGO stages. In the logistic regression model, a statistically significant association was observed at D1-2 between AKI and CD10CD16 immature neutrophils (OR 3.03 [1.7-5.5]-p < 0.001). At D5-7, increased interleukin-10 (IL-10) levels and reduced ex vivo TNF-α production after LPS stimulation were significantly associated with the presence of AKI (OR 1.38 [1.12-1.71]-p = 0.001 and 0.51 [0.27-0.91]-p = 0.03, respectively). Patients who recovered from AKI between D1-2 and D5-7 compared to patients with persistent AKI at D5-7, tended to correct these alterations.
Following various types of severe injuries, early AKI is associated with the initial inflammatory response. Presence of AKI at the end of the first week after injury is associated with injury-induced immunosuppression.
急性肾损伤(AKI)在住院患者中很常见,会导致显著的发病率和死亡率。本研究的目的是探讨重症监护病房患者全身免疫反应,特别是各种类型损伤(脓毒症、创伤、手术和烧伤)后入院后第一周内 AKI 持续存在与免疫特征之间的关系。
REALAKI 是 REAnimation Low Immune Status Marker(REALISM)队列研究的辅助分析,其中 359 名危重症患者被纳入三个不同的重症监护病房。排除了终末期肾病患者。临床样本和数据在入院后三次采集:入院第 1 或 2 天(D1-2)、第 3 或 4 天(D3-4)以及第 5、6 或 7 天(D5-7)。比较了出现 AKI 与未出现 AKI 的患者之间的免疫特征。在 D1-2 和 D5-7 均出现 AKI 的患者被定义为持续 AKI。采用多变量逻辑回归模型确定 AKI 与患者免疫参数之间的独立关联。
本分析共纳入 359 名患者。其中,137 名(38%)为创伤患者,103 名(29%)为术后患者,95 名(26%)为脓毒症患者,24 名(7%)为烧伤患者。139 名(39%)患者在 D1-2 出现 AKI,61 名(20%)在 D5-7 出现 AKI。总体而言,94%的患者在 D5-7 时出现持续 AKI。出现 AKI 的患者表现出促炎和抗炎细胞因子增加,固有和适应性免疫反应改变。在免疫特征中观察到的改变随着 KDIGO 分期的增加而趋于更加明显。在逻辑回归模型中,在 D1-2 时观察到 AKI 与 CD10CD16 不成熟中性粒细胞之间存在统计学显著关联(OR 3.03 [1.7-5.5]-p<0.001)。在 D5-7 时,白细胞介素-10(IL-10)水平升高和脂多糖刺激后 TNF-α产生减少与 AKI 的存在显著相关(OR 1.38 [1.12-1.71]-p=0.001 和 0.51 [0.27-0.91]-p=0.03)。与 D5-7 时持续 AKI 的患者相比,D1-2 至 D5-7 期间从 AKI 中恢复的患者,这些改变有纠正的趋势。
在各种严重损伤后,早期 AKI 与初始炎症反应有关。损伤后第一周结束时出现 AKI 与损伤诱导的免疫抑制有关。